Canonical Allele Identifier: CA2260544256

Gene: MLX

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42571722A= , CM000679.2:g.42571722A=	GRCh38
NC_000017.10:g.40723740A= , CM000679.1:g.40723740A=	GRCh37
NC_000017.9:g.37977266A=	NCBI36
NG_029442.1:g.9663A=
NG_031960.1:g.11110T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435881.7:c.*119A= MANE Select	ENSP00000416627.1:n.*119A=
ENST00000246912.8:c.*119A=	ENSP00000246912.3:n.*119A=
ENST00000346833.8:c.*119A=	ENSP00000320913.3:n.*119A=
ENST00000435881.6:c.*119A=	ENSP00000416627.1:n.*119A=
ENST00000585403.5:n.1061A=
ENST00000588320.1:n.1330A=
ENST00000590050.5:n.1020A=
NM_170607.2:c.*119A=	NP_733752.1:n.*119A=
NM_198204.1:c.*119A=	NP_937847.1:n.*119A=
NM_198205.1:c.*119A=	NP_937848.1:n.*119A=
NM_198204.2:c.*119A= MANE Select	NP_937847.1:n.*119A=
NM_170607.3:c.*119A=	NP_733752.1:n.*119A=
NM_198205.2:c.*119A=	NP_937848.1:n.*119A=